Emerys Elements of Medical Genetics 14th Edition Turnpenny Test Bank

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Product details:

• ISBN-10 ‏ : ‎ 9780702040436
• ISBN-13 ‏ : ‎ 978-0702040436
• Author:  Peter D Turnpenny;  Sian Ellard

Master the genetics you need to know with the updated 14th Edition of Emery’s Elements of Medical Genetics by Drs. Peter Turnpenny and Sian Ellard. Review the field’s latest and most important topics with user-friendly coverage designed to help you better understand and apply the basic principles of genetics to clinical situations. Learning is easy with the aid of clear, full-color illustrative diagrams, a wealth of clinical photographs of genetic diseases, multiple-choice and case-based review questions, end-of-chapter summaries, and convenient online access at www.studentconsult.com. With this highly visual, award-winning classic in your hands, you have all the genetics knowledge you need for exams or practice.

Table of contents:

• Further Reading
• Section A: The Scientific Basis of Human Genetics
• 2. The Cellular and Molecular Basis of Inheritance
• Abstract
• The Cell
• DNA: The Hereditary Material
• Chromosome Structure
• Types of DNA Sequence
• Transcription
• Translation
• The Genetic Code
• Regulation of Gene Expression
• RNA-Directed DNA Synthesis
• Mutations
• Mutations and Mutagenesis
• Further Reading
• 3. Chromosomes and Cell Division
• Abstract
• Human Chromosomes
• Methods of Chromosome Analysis
• Molecular Cytogenetics
• Chromosome Nomenclature
• Cell Division
• Gametogenesis
• Chromosome Abnormalities
• Further Reading
• 4. Finding the Cause of Monogenic Disorders by Identifying Disease Genes
• Position-Independent Identification of Human Disease Genes
• Positional Cloning
• The Human Genome Project
• Identifying the Genetic Etiology of Monogenic Disorders by Next-Generation Sequencing
• Further Reading
• 5. Laboratory Techniques for Diagnosis of Monogenic Disorders
• Abstract
• Polymerase Chain Reaction
• Application of DNA Sequence Polymorphisms
• Nucleic Acid Hybridization Techniques
• Mutation Detection
• Sequencing-Based Methods
• Dosage Analysis
• Genome Sequencing as a Clinical Diagnostic Test
• Further Reading
• 6. Patterns of Inheritance
• Abstract
• Family Studies
• Mendelian Inheritance
• Multiple Alleles and Complex Traits
• Anticipation
• Mosaicism
• Uniparental Disomy
• Genomic Imprinting
• Mitochondrial Inheritance
• Further Reading
• 7. Population and Mathematical Genetics
• Abstract
• Allele Frequencies in Populations
• Genetic Polymorphism
• Segregation Analysis
• Genetic Linkage
• Medical and Societal Intervention
• Conclusion
• Further Reading
• 8. Risk Calculation
• Abstract
• Probability Theory
• Autosomal Dominant Inheritance
• Autosomal Recessive Inheritance
• X-Linked Recessive Inheritance
• The Use of Linked Markers
• Bayes’ Theorem and Prenatal Screening
• Empiric Risks
• Further Reading
• 9. Developmental Genetics
• Abstract
• Fertilization and Gastrulation
• Developmental Gene Families
• The Pharyngeal Arches
• The Role of Cilia in Developmental Abnormalities
• The Limb as a Developmental Model
• Developmental Genes and Cancer
• Positional Effects and Developmental Genes
• Hydatidiform Moles
• Epigenetics and Development
• Sex Determination and Disorders of Sex Development
• Twinning
• Further Reading
• Section B: Genetics in Medicine and Genomic Medicine
• 10. Common Disease, Polygenic, and Multifactorial Genetics
• Types and Mechanisms of Genetic Susceptibility
• Approaches to Demonstrating Genetic Susceptibility to Common Diseases
• Polygenic Inheritance and the Normal Distribution
• Multifactorial Inheritance—the Liability/Threshold Model
• Identifying Genes That Cause Multifactorial Disorders
• Polygenic Risk Scores
• Disease Models for Multifactorial Inheritance
• Further Reading
• 11. Screening for Genetic Disease
• Abstract
• Screening Those at High Risk
• Carrier Testing for Autosomal Recessive and X-Linked Disorders
• Presymptomatic Diagnosis of Autosomal Dominant Disorders
• Ethical Considerations in Carrier Detection and Predictive Testing
• Population Screening
• Criteria for a Screening Program
• Prenatal and Postnatal Screening
• Population Carrier Screening
• Genetic Registers
• Further Reading
• Websites
• 12. Hemoglobin and the Hemoglobinopathies
• Abstract
• Structure of Hemoglobin
• Developmental Expression of Hemoglobin
• Globin Chain Structure
• Synthesis and Control of Hemoglobin Expression
• Disorders of Hemoglobin
• Clinical Variation of the Hemoglobinopathies
• Antenatal and Newborn Hemoglobinopathy Screening
• Further Reading
• Websites
• 13. Immunogenetics
• Abstract
• Immunity
• Innate Immunity
• Specific Acquired Immunity
• Inherited Immunodeficiency Disorders
• Blood Groups
• Further Reading
• 14. The Genetics of Cancer…and Cancer Genetics
• Abstract
• Differentiation Between Genetic and Environmental Factors in Cancer
• Oncogenes
• Tumor Suppressor Genes
• Epigenetics and Cancer
• Genetics of Common Cancers
• DNA Tumor Profiling, Mutational Signatures, and Tumor Mutational Burden
• Inherited Cancer Syndromes
• Genetic Counseling in Familial Cancer
• Screening for Familial Cancer
• What Treatment Is Appropriate?
• Further Reading
• 15. Pharmacogenomics, Precision Medicine, and the Treatment of Genetic Disease
• Pharmacogenomics
• Drug Metabolism
• Genetic Variations Revealed by the Effects of Drugs
• Precision Medicine
• Treatment of Genetic Disease
• Therapeutic Applications of Recombinant DNA Technology
• Gene Therapy
• RNA Modification
• Targeted Gene Correction
• Stem Cell Therapy
• Further Reading
• Section C: Clinical Genetics, Counseling, and Ethics
• 16. Congenital Abnormalities, Dysmorphic Syndromes, and Intellectual Disability
• Abstract
• Incidence
• Definition and Classification of Birth Defects
• Genetic Causes of Malformations
• Environmental Agents (Teratogens)
• Malformations of Unknown Cause
• Counseling
• Intellectual Disability
• Further Reading
• 17. Chromosome Disorders
• Abstract
• Incidence of Chromosome Abnormalities
• Disorders of the Sex Chromosomes
• “Classic” Chromosome Deletion Syndromes
• Chromosome Microarray/Microarray-Comparative Genomic Hybridization
• Chromosome Disorders and Behavioral Phenotypes
• Chromosome Breakage Syndromes
• Indications for Chromosome Microarray Analysis
• Further Reading
• 18. Inborn Errors of Metabolism
• Abstract
• Disorders of Amino Acid and Peptide Metabolism
• Disorders of Carbohydrate Metabolism
• Disorders of Steroid Metabolism
• Disorders of Lipid and Lipoprotein Metabolism
• Lysosomal Storage Disorders
• Disorders in the Metabolism of Purines, Pyrimidines, and Nucleotides
• Disorders of Porphyrin and Heme Metabolism
• Disorders in the Metabolism of Trace Elements and Metals
• Peroxisomal Disorders
• Disorders of Fatty Acid and Ketone Body Metabolism
• Disorders of Energy Metabolism
• Prenatal Diagnosis of Inborn Errors of Metabolism
• Further Reading
• 19. Mainstream Monogenic Disorders
• Abstract
• Neurological Disorders
• CADASIL and Early-Onset Dementia
• Inherited Peripheral Neuropathies
• Motor Neurone Disease
• Neurocutaneous Disorders
• Muscular Dystrophies
• Respiratory Disorders
• Inherited Cardiac Conditions
• Connective Tissue Disorders
• Renal Disorders
• Blood Disorders
• Further Reading
• 20. Prenatal Testing and Reproductive Genetics
• Abstract
• Techniques Used in Prenatal Diagnosis
• Antenatal and Prenatal Screening
• Indications for Prenatal Testing
• Special Problems in Prenatal Diagnosis
• Termination of Pregnancy
• Preimplantation Genetic Diagnosis
• Assisted Conception and Implications for Genetic Disease
• Prenatal Treatment
• Further Reading
• 21. Genetic Counseling
• Abstract
• Definition
• Establishing the Diagnosis
• Calculating and Presenting the Risk
• Discussing the Options
• Communication and Support
• Genetic Counseling—Directive or Non-directive?
• Outcomes in Genetic Counseling
• Special Issues in Genetic Counseling
• Further Reading

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